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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919169Generated: October 31, 2026

Trifluoromethylsulfinylchloride → 5-amino-1-(2-chloro-6-fluoro-4-(trifluoromethyl)phenyl)-4-(trifluoromethylsulfinyl)-1H-pyrazole-3-carbonitrile

https://huagongshe.com/reaction/919169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethylsulfinylchlorideHCID 11008121—
ReactantDimethylamine p-toluenesulfonateHCID 12199009—
Reactant5-amino-1-(2-chloro-6-fluoro-4-(trifluoromethyl)-phenyl)-1H-pyrazole-3-carbonitrileHCID 68409371—
SolventTolueneHCID 1140—
Product5-amino-1-(2-chloro-6-fluoro-4-(trifluoromethyl)phenyl)-4-(trifluoromethylsulfinyl)-1H-pyrazole-3-carbonitrileHCID 8985879064.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 5-amino-1-(2-chloro-6-fluoro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile (140 g, 459.6 mmol, 1.00 eq.) and dimethylamine tosylate (151.8 g, 698.6 mmol, 1.52 eq.) in toluene (840 mL) was added CF3SOCl (89.7 g, 588.3 mmol, 1.28 eq.). After the mixture was stirred at 40° C. for 16 h, nitrogen was bubbled through the solution and the solution was cooled to rt. Then the mixture was poured into 2 L ice/water and stirred at 0° C. for 1 h. The precipitated solid was isolated by filtration and dried under vacuum. The solid was recrystallized with toluene to give 5-amino-1-(2-chloro-6-fluoro-4-(trifluoromethyl)phenyl)-4-(trifluoromethylsulfinyl)-1H-pyrazole-3-carbonitrile (125 g, 64%) as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273007B2
Source datasetuspto-grants-2016_03
ORD IDord-9dac93fa030f492ba721f2b855d99919
Source noteuspto-grants-2016_03